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About This Item
Linear Formula:
CH3(CH2)12COCl
CAS Number:
Molecular Weight:
246.82
EC Number:
203-994-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
636924
MDL number:
Assay:
≥99%
Form:
liquid
assay
≥99%
form
liquid
refractive index
n20/D 1.449 (lit.)
bp
250 °C/100 mmHg (lit.)
mp
−1 °C (lit.)
density
0.908 g/mL at 25 °C (lit.)
storage temp.
−20°C
SMILES string
CCCCCCCCCCCCCC(Cl)=O
InChI
1S/C14H27ClO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3
InChI key
LPWCRLGKYWVLHQ-UHFFFAOYSA-N
Biochem/physiol Actions
Covalent attachment of myristate is a common occurrence on a wide variety of viral and cellular proteins and plays a role in promoting membrane binding.
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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J Goldberg
Cell, 95(2), 237-248 (1998-10-28)
Ras-related GTPases are positively regulated by guanine nucleotide exchange factors (GEFs) that promote the exchange of GDP for GTP. The crystal structure of the Sec7 domain GEF bound to nucleotide-free ARF1 GTPase has been determined at 2.8 A resolution and
M D Resh
Biochimica et biophysica acta, 1451(1), 1-16 (1999-08-14)
Covalent attachment of myristate and/or palmitate occurs on a wide variety of viral and cellular proteins. This review will highlight the latest advances in our understanding of the enzymology of N-myristoylation and palmitoylation as well as the functional consequences of
Janclei P Coutinho et al.
Talanta, 134, 256-263 (2015-01-27)
In this work a multivariate statistical tool (Derringer and Suich optimization) was proposed for the separation of seventeen capsinoids (natural and synthetic) using the UHPLC-DAD chromatography. Capsinoids were analyzed at 280 nm. The variables optimized were the mobile phase (water
